Lacey C B, Elde R P, Seybold V S
Department of Cell Biology and Neuroanatomy, University of Minnesota, Minneapolis 55455.
Peptides. 1991 Mar-Apr;12(2):383-91. doi: 10.1016/0196-9781(91)90030-s.
The purpose of this study was to determine the distribution of VIP binding sites in the thymus and bursa of Fabricius using receptor binding and autoradiographic techniques. Biochemical characterization of 125I-VIP binding sites determined two classes of specific binding sites in both tissues. The dissociation constants determined in the thymus were 1.12 nM and 88.5 nM, and in the bursa were 0.459 nM and 70.8 nM. Autoradiographic localization of 125I-VIP binding sites within the thymus demonstrated specific binding associated with the medullary region of the thymic lobule and the blood vessels in the interlobular and trabecular areas. Within the bursa of Fabricius, high densities of silver grains corresponded with vascular elements in the interfollicular regions, the epithelial border of the plicae, the muscular layer surrounding the organ, and the diffusely infiltrated area near the burso-cloacal duct.
本研究的目的是使用受体结合和放射自显影技术确定胸腺和法氏囊中血管活性肠肽(VIP)结合位点的分布。对125I-VIP结合位点的生化特性分析确定了两种组织中均存在两类特异性结合位点。在胸腺中测得的解离常数分别为1.12 nM和88.5 nM,在法氏囊中测得的解离常数分别为0.459 nM和70.8 nM。125I-VIP结合位点在胸腺内的放射自显影定位显示,特异性结合与胸腺小叶的髓质区域以及小叶间和小梁区域的血管有关。在法氏囊中,高密度的银颗粒与滤泡间区域的血管成分、皱襞的上皮边界、器官周围的肌肉层以及法氏囊-泄殖腔管附近的弥漫浸润区域相对应。